Catastrophic Antiphospholipid Syndrome in a Lupus Patient With Severe Recurrent Life-Threatening Clinical Manifestations.

Journal of medical cases Pub Date : 2024-10-01 Epub Date: 2024-09-20 DOI:10.14740/jmc4255
Abdulrahman Ali M Khormi, Maged Ba Gunaid, Mohammed Fayyad, Mostafa Mohrag, Ali Abdullah AlAseeri
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引用次数: 0

Abstract

Catastrophic antiphospholipid syndrome (CAPS) is a rare, severe, and life-threatening form of antiphospholipid syndrome (APS). Early recognition and rapid treatment are of great importance to improve patient outcomes and decrease mortality. Herein, we present a case of lupus and APS with obstetric complications, recurrent thrombosis, and renal and hematological manifestations of APS which showed great response to the treatment.

一名红斑狼疮患者出现严重的抗磷脂综合征,并反复出现危及生命的临床表现。
重症抗磷脂综合征(CAPS)是一种罕见、严重且危及生命的抗磷脂综合征(APS)。早期识别和快速治疗对于改善患者预后和降低死亡率至关重要。在此,我们介绍了一例狼疮合并 APS 病例,该患者伴有产科并发症、复发性血栓形成以及 APS 的肾脏和血液学表现,且对治疗反应良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.10
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